Journal of Colloid and Interface Science, Vol.294, No.1, 95-103, 2006
Destabilization of polystyrene latex particles induced by adsorption of polyvinylamine: Mass, size and structure characteristics of the growing aggregates
The obviously visible aggregation of suspended colloidal particles resulting from the addition of polyvinylamine to the aqueous dispersion of polystyrene latex particles bearing surface sulfate groups set in with a delay of 24 h. The aggregation mechanisms and the fractal dimension of the aggregates were derived from the variations with time of the weight and number averaged masses of the aggregates as well as of the weight averaged harmonic mean diameter of the size distribution. Since the establishment of starved layers was determined to be relatively fast and to leave the liquid phase free of polymer, the delay for the obvious destabilization was attributed to the reconformation of adsorbed macromolecules that was expected to be extremely slow. This reconformation promoted the emergence of the diffusion-limited aggregation process that accompanies the permanent reaction-limited aggregation process. The fractal dimension of the latex particles/polyvinylarnine aggregates was determined to be 2.12. (c) 2005 Elsevier Inc. All rights reserved.
Keywords:polyvinylamine;polyvinylamine adsorption;polymer-induced diffusion-limited aggregation;polymer-induced reaction-limited aggregation;fractal dimension;particle counting;particle sizing